A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053112



Internal ID21962346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97185384..97185384hg38UCSC Ensembl
chrX:96440383..96440383hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642067
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053112
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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